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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Spheroid body myopathy
Extraskeletal myxoid chondrosarcoma

MYOT EWSR1
NR4A3
TAF15
TCF12
TFG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYOT
(0.63)
TFG



Citations in the biomedical literature:


Spheroid body myopathy
MYOT
Extraskeletal myxoid chondrosarcoma
EWSR1 NR4A3 TAF15 TCF12 TFG



Spheroid body myopathy
Extraskeletal myxoid chondrosarcoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.